Related Experiment Video
Updated: Aug 14, 2026

Comprehensive Profiling of Dopamine Regulation in Substantia Nigra and Ventral Tegmental Area
Published on: August 10, 2012
Does cholecystokinin potentiate dopamine action in the nucleus accumbens?
Abstract:
Extracellular single unit recording and microiontophoretic techniques were used to determine whether sulfated cholecystokinin octapeptide (CCK-8S) potentiates the inhibitory action of dopamine (DA) on neurons in the nucleus accumbens of rats. The results show that CCK-8S attenuated, rather than enhanced the action of DA. The interaction between CCK-8S and DA does not appear to be specific because similar antagonizing actions between CCK-8S and serotonin were observed. In addition to opposing the inhibitory effects of DA and serotonin, CCK-8S potentiated the activation of glutamate. It is concluded that CCK-8S and DA exerted their actions independently via depolarizing and hyperpolarizing the neuronal membrane of the NAc neurons, respectively.
More Related Videos
08:07Simultaneous Detection of c-Fos Activation from Mesolimbic and Mesocortical Dopamine Reward Sites Following Naive Sugar and Fat Ingestion in Rats
Published on: August 24, 2016
06:40Combined Infusion and Stimulation with Fast-Scan Cyclic Voltammetry (CIS-FSCV) to Assess Ventral Tegmental Area Receptor Regulation of Phasic Dopamine
Published on: April 23, 2020
Related Concept Videos
Direct-Acting Cholinergic Agonists: Pharmacokinetics
Drugs Acting on Autonomic Ganglia: Stimulants
Ganglionic stimulants activate NM nicotinic receptors in autonomic ganglia, falling into two categories: nicotine mimetics [e.g., lobeline, dimethylpiperazine, tetramethylammonium] and muscarinic receptor agonists [e.g., muscarine, methacholine]. The first category's action is rapid and blocked by nicotinic receptor antagonists, while the second category's action is delayed and blocked by atropine-like agents. Nicotine, an alkaloid, affects the heart rate by stimulating sympathetic or...
Adrenergic Agonists: Indirect-Acting Agents
One mechanism involves depleting stored catecholamines by displacing them from synaptic vesicles. These agents, known as "displacers," are transported into vesicles at the expense of noradrenaline. Examples include amphetamine and tyramine, which lack a catechol moiety, resulting in prolonged action, improved oral bioavailability, and...
Drugs Affecting Neurotransmitter Synthesis
Drugs Affecting GI Tract Motility: Dopamine Receptor Antagonists
Chemotherapy-Induced Nausea and Vomiting: Dopamine Receptor Antagonists
Phenothiazines, such as prochlorperazine...